Sequence-specific resonance assignment and secondary structure of (1-71) bacterioopsin.

Abstract:

:The conformation of chymotryptic fragment C2 of bacteriohodopsin (residues 1-71) was studied by 2D 1H NMR. The fragment was solubilized in a mixture of chloroform/methanol (1:1), 0.1 M LiClO4. Most of the resonances in 1H NMR spectra of fragment C2 were assigned using phase-sensitive DQF-COSY, TOCSY, and NOESY techniques. To simplify the assignment procedure for overlapping regions of NMR spectra, an analog of fragment C2 with leucines deuterated in beta-positions was used. Deuterium exchange rates for amide protons were measured in a series of TOCSY spectra. Two right-handed alpha-helical regions Pro8-Lys30 and Lys41-Leu62 were identified on the basis of NOE connectivities and deuterium exchange rates. The N-terminal part of the fragment (Ala2-Gly6) adopts the helical conformation stabilized by 3 hydrogen bonds.

journal_name

J Biomol NMR

authors

Sobol AG,Arseniev AS,Abdulaeva GV,Musina LYu,Bystrov VF

doi

10.1007/BF01875527

subject

Has Abstract

pub_date

1992-03-01 00:00:00

pages

161-71

issue

2

eissn

0925-2738

issn

1573-5001

journal_volume

2

pub_type

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